Congenital Zika Syndrome
What's New
Last Posted: Aug 08, 2023
- Investigation of the impact of AXL, TLR3, and STAT2 in congenital Zika syndrome through genetic polymorphisms and protein-protein interaction network analyses.
Julia A Gomes, et al. Birth defects research 2023 0 - Association between genetic variants in TREM1, CXCL10, IL4, CXCL8 and TLR7 genes with the occurrence of congenital Zika syndrome and severe microcephaly.
Santos Camilla Natália Oliveira, et al. Scientific reports 2023 0 (1) 3466 - Association Between Zika Virus Microcephaly in Newborns With the rs3775291 Variant in Toll-Like Receptor 3 and rs1799964 Variant at Tumor Necrosis Factor-? Gene.
Santos Camilla N O, et al. The Journal of infectious diseases 2019 0 (11) 1797-1801 - Contribution of miR-124 rs531564 polymorphism to the occurrence of congenital Zika syndrome.
Gomes Julia A, et al. Epigenetics 2022 0 1-7 - Congenital Zika Syndrome Is Associated With Interferon Alfa Receptor 1.
Azamor Tamiris, et al. Frontiers in immunology 2021 0 764746 - Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome.
Borda Victor, et al. PLoS neglected tropical diseases 2021 0 (6) e0009507 - Association between Maternal Non-Coding Interferon-? Polymorphisms and Congenital Zika Syndrome in a Cohort from Brazilian Northeast.
Rossi Átila Duque, et al. Viruses 2021 11 (11) - Functional Polymorphisms in the p53 Pathway Genes on the Genetic Susceptibility to Zika Virus Teratogenesis.
Gomes Julia A, et al. Frontiers in cellular and infection microbiology 2021 0 641413 - Association between Genetic Variants in NOS2 and TNF Genes with Congenital Zika Syndrome and Severe Microcephaly.
Gomes Julia A, et al. Viruses 2021 0 (2) - Why is congenital Zika syndrome asymmetrically distributed among human populations?
Barbeito-Andrés Jimena et al. PLoS biology 2018 Aug (8) e2006592
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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